RGS8 regulator of G protein signaling 8
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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18 |
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0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
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Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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MIM | 607189 OMIM |
HGNC | HGNC:16810 HGNC |
Ensembl | ENSG00000135824 Ensembl |
AllianceGenome | HGNC:16810 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000515211.2 | hg38 | chr1 | 182,641,818 | 182,684,587 | 42,770 |
ENST00000483095.6 | hg38 | chr1 | 182,646,104 | 182,671,929 | 25,826 |
ENST00000258302.8 | hg38 | chr1 | 182,641,816 | 182,672,914 | 31,099 |
ENST00000367556.5 | hg38 | chr1 | 182,646,735 | 182,671,853 | 25,119 |
ENST00000367557.8 | hg38 | chr1 | 182,646,686 | 182,672,908 | 26,223 |
ENST00000258302.8 | hg19 | chr1 | 182,610,951 | 182,642,049 | 31,099 |
ENST00000515211.2 | hg19 | chr1 | 182,610,953 | 182,653,722 | 42,770 |
ENST00000483095.6 | hg19 | chr1 | 182,615,239 | 182,641,064 | 25,826 |
ENST00000367557.8 | hg19 | chr1 | 182,615,821 | 182,642,043 | 26,223 |
ENST00000367556.5 | hg19 | chr1 | 182,615,870 | 182,640,988 | 25,119 |
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